Mab-21 like 1 is a protein that in humans is encoded by the MAB21L1 gene. [5]

MAB21L1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesMAB21L1, CAGR1, Nbla00126, mab-21 like 1, COFG
External IDsOMIM: 601280; MGI: 1333773; HomoloGene: 36183; GeneCards: MAB21L1; OMA:MAB21L1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_005584

NM_010750

RefSeq (protein)

NP_005575

NP_034880

Location (UCSC)Chr 13: 35.47 – 35.48 MbChr 3: 55.69 – 55.69 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

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This gene is similar to the MAB-21 cell fate-determining gene found in C. elegans. It may be involved in eye and cerebellum development, and it has been proposed that expansion of a trinucleotide repeat region in the 5' UTR may play a role in a variety of psychiatric disorders. [provided by RefSeq, Oct 2008].

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000180660Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000056947Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: Mab-21 like 1". Retrieved 2020-04-12.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.